Study in Adult Patients With Moderate to Severe Asthma

Asthma Clinical Trial

— FEEL  

Official title:

An Exploratory, Double-blind, Randomised, Multicenter, Psychopharmacological Study in Adult Patients With Moderate to Severe Asthma to Compare Two Pressurised Metered-Dose Inhalers (pMDIs) on Patients' Perception of Asthma Symptoms

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04886999
• Other study ID #: CLI-01535AA0-02
• Secondary ID: 2021-001449-11
• Status: Completed
• Phase: Phase 3
• Start date: February 24, 2022
• Est. completion date: February 1, 2023

Study information

• Verified date: February 2024
• Source: Chiesi Farmaceutici S.p.A.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The CLI-01535AA02-2 Study is an exploratory study designed to compare two pressurised metered Dose inhalers on subject's perception of asthma symptoms.

Description:

Outpatients attending the hospital clinics/study centers will be recruited. Moderate to severe asthma adult subjects will be recruited. A total of 75 subjects will be enrolled. The whole study will last approximately 6 weeks for each subject.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 78
• Est. completion date: February 1, 2023
• Est. primary completion date: February 1, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Subject's and/or subject legal representative's written informed consent obtained prior to any study related procedure.

• Age: =18 and =75 years of age.

• Established diagnosis of permanent asthma for at least 6 months prior to screening/randomisation visit

• Subject on maintenance therapy treated by Foster® (CHF1535 100/6 µg pMDI) for at least 6 months prior to screening/randomisation visit

• Asthma Control Test (ACT) = 20 at screening/randomisation visit.

• Subject must have a cooperative attitude and the ability to be trained to use correctly the diary and answer the Visual Analogue Scale (VAS)

• Subject willing and able to download the application on their personal electronic device to fill in the study e-diary.

• Female subject of non-childbearing potential defined as physiologically incapable of becoming pregnant or female subject + male Partner must be willing to use a highly effective birth control method from the signature of the informed consent and until Visit 4

Exclusion Criteria:

• Pregnant or lactating woman

• History of 'at risk' asthma

• Recent exacerbation

• Non-permanent asthma

• Asthma requiring more than 1 inhaler for maintenance treatment and more than 1 inhaler for reliever treatment.

• Asthma requiring use of biologics

• Respiratory disorders

• Lower tract respiratory infection

• Current smoker or ex-smoker with a smoking current use/history of = 10 pack-years

• Cardiovascular diseases

• subject with historical or current evidence of uncontrolled concurrent disease such as but not limited to hyperthyroidism, diabetes mellitus or other endocrine disease; haematological disease; autoimmune disorders

• Alcohol/drug abuse

Related Conditions & MeSH terms

• Asthma

Intervention

Behavioral:
• Exploratory study on patient's perception of Asthma symptoms
To assess the perception of symptoms and the psychopharmacological aspects in patients with moderate to severe asthma comparing two inhalers of CHF1535 100/6 µg pMDI

Locations

Country	Name	City	State
Italy	Chiesi 38011	Bari
Italy	Chiesi 38009	Battipaglia
Italy	Chiesi 38006	Cagliari
Italy	Chiesi 38010	Catanzaro
Italy	Chiesi 38003	Genova
Italy	Chiesi 38001	Milan
Italy	Chiesi 38005	Napoli
Italy	Chiesi 38004	Palermo
Italy	Chiesi 38002	Roma
Italy	Chiesi 38007	Sassari

Sponsors (1)

Lead Sponsor	Collaborator
Chiesi Farmaceutici S.p.A.

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Summary measures (for questions with continuous outcome) to report patients' expectations of their symptoms change at Day 15 (Visit 2)	Assessed by Visual Analogue Scale (VAS) that ranges from 0 to 100. When question refers to symptom improvement, higher score means better outcome. When question refers to symptoms worsening, higher score means worse outcome.; Each question will be analysed separately.	At Day 15 (Visit 2)
Primary	Summary measures (for questions with continuous outcome) to report patients' expectations of their symptoms change at Day 29 (Visit 3)	Assessed by Visual Analogue Scale (VAS) that ranges from 0 to 100. When question refers to symptom improvement, higher score means better outcome. When question refers to symptoms worsening, higher score means worse outcome.; Each question will be analysed separately.	At Day 29 (Visit 3)
Primary	Summary measures (for questions with continuous outcome) to report patients' expectations of their symptoms change at Day 43 (Visit 4)	Assessed by Visual Analogue Scale (VAS) that ranges from 0 to 100. When question refers to symptom improvement, higher score means better outcome. When question refers to symptoms worsening, higher score means worse outcome.; Each question will be analysed separately.	At Day 43 (Visit 4)
Primary	Percentages of subjects (for questions with categorical outcome) to evaluate patients' preference of device at Day 43 (Visit 4)	Questions covering patients' preference of device and outcome assessments will be reported on the ITT and PP set by treatment group. This analysis will be applied on questions not collected daily. Each question will be analysed separately.	At Day 43 (Visit 4)
Primary	Percentages of subjects (for questions with categorical outcome) to evaluate patients' perception of inhalers changes at Day 43 (Visit 4)	Questions covering patients' preference of device and outcome assessments will be reported on the ITT and PP set by treatment group. This analysis will be applied on questions not collected daily. Each question will be analysed separately.	At Day 43 (Visit 4)
Primary	Change from baseline in average Visual Analogic Scale score of subjects' perceptions of asthma symptoms after 14 days of treatment	Visual Analogue Scale (VAS) ranges from 0 to 100. When question refers to symptom improvement, higher score means better outcome. When question refers to symptoms worsening, higher score means worse outcome.	After 14 days of treatment
Primary	Change from baseline in average Visual Analogic Scale score of subjects' perceptions of asthma symptoms after the first 7 days of treatment	Visual Analogue Scale (VAS) ranges from 0 to 100. When question refers to symptom improvement, higher score means better outcome. When question refers to symptoms worsening, higher score means worse outcome.	After the first 7 days of treatment
Primary	Change from baseline in rescue medication use	To be summarised on the "Intention To Treat" set by treatment group by descriptive statistics. Baseline value is defined as the average value (puffs/day) collected during the baseline period.	After 14 days of treatment
Primary	Change from baseline in Asthma Quality of Life Questionnaire (AQLQ) score	There are 32 questions in the AQLQ that are divided in 4 domains (symptoms, activity limitation, emotional function and environmental stimuli). Answers are done on a 7-point scale (7 = not impaired at all - 1 = severely impaired), with higher scores indicating better quality of life.	After 14 days of treatment
Secondary	Occurrence of Treatment Emergent Adverse Event (TEAEs), adverse drug reactions (ADRs), severe ADRs, serious ADRs, serious TEAEs (Serious Adverse Events), non-serious TEAEs, severe TEAEs	Occurrence of Treatment Emergent Adverse Event (TEAEs), adverse drug reactions (ADRs), severe ADRs, serious ADRs, serious TEAEs (Serious Adverse Events), non-serious TEAEs, severe TEAEs, TEAEs leading to discontinuation from study treatment and TEAEs leading to death.; Summarised on the safety set by treatment group as the number of subjects, percentage of subjects, and number of events. All adverse events starting on or after the time of first study drug intake will be classified as TEAE. Any adverse events started after the informed consent signature and before the time of first study drug intake will be classified as pre-treatment adverse event.	From date of the first study drug intake unil date of study treatment, or date of death or up to 14 days after date of the last study drug intake, whichever came first

External Links

•   Study Record on EU Clinical Trials Register including results